Answer:
Dude im not 100% sure but I think its b and c im sorry if im wrong its just that im not really sure which ones are.
Explanation:
Note the signs of equilibrium:-
- Reaction don't procede forward or backward
- Concentration of products and reactants remains same .
So
if
Concentration of A is 2M then concentration of B should be same .
So equilibrium constant K is 1
![\\ \rm\rightarrowtail K=\dfrac{[Products]^a}{[Reactants]^b}](https://tex.z-dn.net/?f=%5C%5C%20%5Crm%5Crightarrowtail%20K%3D%5Cdfrac%7B%5BProducts%5D%5Ea%7D%7B%5BReactants%5D%5Eb%7D)
So
Explanation:
- As it is given that boiling point of propanamide is very high. So, reason for this is that easy formation of hydrogen bonds which are strong enough that we have to provide large amount of heat to break it.
As in
, the hydrogen atoms which are present are positive in nature. Due to this they are able to form hydrogen bonds with the neighboring oxygen atom.
Hence, these bonds are so strong that high heat needs to given to break them.
- A propanoic acid contain carboxylic group as the functional group. So, this group is also able to form hydrogen bonding as it forms a hydrogen bond between an acid group and hydroxyl group of neighboring molecule.
Hence, it will also require high heat to break the bond due to which there will be increase in boiling point.
- In propanal, there is presence of aldehyde functional group and three carbon atoms chain which will not form strong bonding with the hydrogen atom of CHO. Due to this there will exist weak Vander waal's force that is not at all strong enough.
As a result, less energy will be needed to break the bonds in propanal. Hence, it has very low boiling point.
Answer:
see explanation below
Explanation:
The question is incomplete. The missing parts are a) determine the electrophylic site. b) determine the nucleophylic site.
In order to do this, we need to write the reaction and do the mechanism. The nucleophylic site will be the site where the nucleophyle attacks to form the product. In this case the site is the carbon next to the bromine. In this place the Oxigen which is the nucleophyle goes. The electrophyle is the site where one atom substract to complete it's charges. In this case, the electrophyle is usually the hydrogen, so the site will be next to the oxygen after the nucleophyle attack.
You can see it better in the attached picture.
The answer is D) <span>The Ka is small, and the equilibrium favors reactants.
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